Miloxan Suspensie voor injectie
Miloxan Suspensie voor injectie
Not authorised
- Clostridium chauvoei, Inactivated
- Clostridium tetani, toxoid
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium sordellii, toxoid
- Clostridium perfringens, epsilon toxoid
- Clostridium perfringens, beta toxoid
Product identification
Medicine name:
Miloxan Suspensie voor injectie
Miloxan Suspension injectable
Miloxan Injektionslösung
Active substance:
- Clostridium chauvoei, Inactivated
- Clostridium tetani, toxoid
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium sordellii, toxoid
- Clostridium perfringens, epsilon toxoid
- Clostridium perfringens, beta toxoid
Target species:
-
Sheep
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium chauvoei, Inactivated90.00/percentage protection2.00millilitre(s)
-
Clostridium tetani, toxoid2.50/international unit(s)2.00millilitre(s)
-
Clostridium septicum, toxoid2.50/international unit(s)2.00millilitre(s)
-
Clostridium novyi, toxoid3.50/international unit(s)2.00millilitre(s)
-
Clostridium sordellii, toxoid90.00/percentage protection2.00millilitre(s)
-
Clostridium perfringens, epsilon toxoid5.00/international unit(s)2.00millilitre(s)
-
Clostridium perfringens, beta toxoid10.00/international unit(s)2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Miloxan 250 ml Vial Suspension for injection
- Miloxan 100 ml Vial Suspension for injection
- Miloxan 50 ml Vial Suspension for injection
- Miloxan 4 ml Vial Suspension for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V149037
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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